Global Medical Director responsible for implementing medical strategies globally for Cell & Gene Therapy in Oncology. Leading evidence generation activities and representing Global Medical Affairs with stakeholders.
Responsibilities
Lead development and execution of medical affairs strategy for Oncology Cell & Gene priority programs including transformative tactics such as: research/population health, innovative partnerships and integrated evidence plans
Co-develop plans for evidence generation, Medical Science Liaison (MSL) / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with (TAs)
Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders
Financial tracking to ensure timely and cost-effective development & execution of medical activities
Prepare Scientific Review Committee submissions for TA assets within remit
Partner with Development, Strategy and growth (S&G), US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs
Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners
Represent “the voice of the patient” internally and evaluate factors relevant to a patient’s informed decision making
Provide direction and input into the development and implementation of successful reimbursement and market-access strategies
Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities.
Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance
Ensures GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards
Provide proactive medical input to asset lifecycle management to consider new therapeutic opportunities
Requirements
MD (Preferred) or PhD/PharmD in Health Sciences.
5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development
Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.
Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change with an agile mindset & ability to lead in an agile organization across Disease Areas
Ability to truly collaborate across functions and markets: serve-partner-co-create
Deep understanding of health care systems and key external stakeholders
Strong track record of delivery focus for time and quality in medical affairs projects with successful development and implementation of innovative programs and processes
Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination.
Benefits
Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Job title
Global Medical Director – Cell & Gene Therapy, Oncology
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